반응식
[CH2:1]([O:4][C:5]1[CH:10]=[CH:9][N+:8]([O-])=[C:7]([CH3:12])[C:6]=1[CH3:13])[CH2:2][CH3:3].[C:14]([O:17]C(=O)C)(=[O:16])[CH3:15]>>[C:14]([O:17][CH2:12][C:7]1[C:6]([CH3:13])=[C:5]([O:4][CH2:1][CH2:2][CH3:3])[CH:10]=[CH:9][N:8]=1)(=[O:16])[CH3:15]참가 물질
3
실험 절차
To 20.3 g of 4-propoxy-2,3-dimethylpyridine-1-oxide, 44.0 g (4.0 eq.) of acetic anhydride was added, and the mixture was allowed to react for 4 hours at 90° C. Acetic anhydride was distilled off, and then the resulting concentrated residue was purified on a silica gel column, to obtain 27.8 g of 2-acetoxymethyl-3-methyl-4-propoxy-pyridine as an oily matter.
후처리
- customto react for 4 hours at 90° C
- distillationAcetic anhydride was distilled off
- customthe resulting concentrated residue was purified on a silica gel column
출처 및 근거
- ORD 기록
- ord-c203c1efd1c54484ab6c0daecdce4cf4
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08778975B2
연결된 노트
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